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spelling todo:paper_10217401_v14_n3-4_p175_Calafat2023-10-03T15:56:37Z NOD mice exocrinopathy: Towards a neuroimmune link Calafat, M. Larocca, L. Roca, V. Pérez Leirós, C. Apoptotic acinar cells Exocrinopathy Macrophages Neuroimmune Nitric oxide NOD mice gamma interferon interleukin 10 lipopolysaccharide nitric oxide nitrite vasoactive intestinal polypeptide acinar cell animal cell animal model apoptosis conference paper controlled study female macrophage mouse nonhuman nonobese diabetic mouse peritoneum macrophage priority journal Sjoegren syndrome stimulation submandibular gland Animals Apoptosis Cells, Cultured Disease Models, Animal Epithelial Cells Epithelium Female Inflammation Mediators Interferon Type II Interleukin-10 Lipopolysaccharides Macrophages Mice Mice, Inbred BALB C Mice, Inbred NOD Neuroimmunomodulation Nitric Oxide Peritoneum Sjogren's Syndrome Submandibular Gland Vasoactive Intestinal Peptide Sjögren's syndrome (SS) is a chronic autoimmune disorder of exocrine glands characterized as an autoimmune exocrinopathy and more specifically as an autoimmune epithelitis. An impaired balance of neuroimmune interactions mediated by vasoactive intestinal peptide (VIP) in the target organ at early stages of disease is explored by means of the nonobese diabetic (NOD) mouse model of SS. We have previously described a reduced salivary secretion and signaling upon VIP stimulation. The effect reflected a differential regulation of the neural isoform of nitric oxide synthase by calcium calmodulin kinase II and occurred prior to the appearance of detectable levels of cytokines in NOD glands. VIP acting on NOD macrophages treated with lipopolysaccharide promoted anti-inflammatory effects by inhibiting nitric oxide synthase induction as well as IL-12 and TNF-α production, while stimulating IL-10. Here we present evidence on the ability of apoptotic acinar cells from submandibular glands of NOD mice to stimulate nitric oxide in both peritoneal and glandular macrophage pools to a similar extent as lipopolysaccharide + IFN-γ. VIP was not effective to prevent nitrite accumulation and modestly increased IL-10 levels in macrophages coincubated with acinar cells. An enhanced nitrite response of NOD glandular macrophages in basal and stimulated conditions compared to peritoneal cells is also shown. Copyright © 2007 S. Karger AG. Fil:Calafat, M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Larocca, L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Roca, V. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Pérez Leirós, C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_10217401_v14_n3-4_p175_Calafat
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Apoptotic acinar cells
Exocrinopathy
Macrophages
Neuroimmune
Nitric oxide
NOD mice
gamma interferon
interleukin 10
lipopolysaccharide
nitric oxide
nitrite
vasoactive intestinal polypeptide
acinar cell
animal cell
animal model
apoptosis
conference paper
controlled study
female
macrophage
mouse
nonhuman
nonobese diabetic mouse
peritoneum macrophage
priority journal
Sjoegren syndrome
stimulation
submandibular gland
Animals
Apoptosis
Cells, Cultured
Disease Models, Animal
Epithelial Cells
Epithelium
Female
Inflammation Mediators
Interferon Type II
Interleukin-10
Lipopolysaccharides
Macrophages
Mice
Mice, Inbred BALB C
Mice, Inbred NOD
Neuroimmunomodulation
Nitric Oxide
Peritoneum
Sjogren's Syndrome
Submandibular Gland
Vasoactive Intestinal Peptide
spellingShingle Apoptotic acinar cells
Exocrinopathy
Macrophages
Neuroimmune
Nitric oxide
NOD mice
gamma interferon
interleukin 10
lipopolysaccharide
nitric oxide
nitrite
vasoactive intestinal polypeptide
acinar cell
animal cell
animal model
apoptosis
conference paper
controlled study
female
macrophage
mouse
nonhuman
nonobese diabetic mouse
peritoneum macrophage
priority journal
Sjoegren syndrome
stimulation
submandibular gland
Animals
Apoptosis
Cells, Cultured
Disease Models, Animal
Epithelial Cells
Epithelium
Female
Inflammation Mediators
Interferon Type II
Interleukin-10
Lipopolysaccharides
Macrophages
Mice
Mice, Inbred BALB C
Mice, Inbred NOD
Neuroimmunomodulation
Nitric Oxide
Peritoneum
Sjogren's Syndrome
Submandibular Gland
Vasoactive Intestinal Peptide
Calafat, M.
Larocca, L.
Roca, V.
Pérez Leirós, C.
NOD mice exocrinopathy: Towards a neuroimmune link
topic_facet Apoptotic acinar cells
Exocrinopathy
Macrophages
Neuroimmune
Nitric oxide
NOD mice
gamma interferon
interleukin 10
lipopolysaccharide
nitric oxide
nitrite
vasoactive intestinal polypeptide
acinar cell
animal cell
animal model
apoptosis
conference paper
controlled study
female
macrophage
mouse
nonhuman
nonobese diabetic mouse
peritoneum macrophage
priority journal
Sjoegren syndrome
stimulation
submandibular gland
Animals
Apoptosis
Cells, Cultured
Disease Models, Animal
Epithelial Cells
Epithelium
Female
Inflammation Mediators
Interferon Type II
Interleukin-10
Lipopolysaccharides
Macrophages
Mice
Mice, Inbred BALB C
Mice, Inbred NOD
Neuroimmunomodulation
Nitric Oxide
Peritoneum
Sjogren's Syndrome
Submandibular Gland
Vasoactive Intestinal Peptide
description Sjögren's syndrome (SS) is a chronic autoimmune disorder of exocrine glands characterized as an autoimmune exocrinopathy and more specifically as an autoimmune epithelitis. An impaired balance of neuroimmune interactions mediated by vasoactive intestinal peptide (VIP) in the target organ at early stages of disease is explored by means of the nonobese diabetic (NOD) mouse model of SS. We have previously described a reduced salivary secretion and signaling upon VIP stimulation. The effect reflected a differential regulation of the neural isoform of nitric oxide synthase by calcium calmodulin kinase II and occurred prior to the appearance of detectable levels of cytokines in NOD glands. VIP acting on NOD macrophages treated with lipopolysaccharide promoted anti-inflammatory effects by inhibiting nitric oxide synthase induction as well as IL-12 and TNF-α production, while stimulating IL-10. Here we present evidence on the ability of apoptotic acinar cells from submandibular glands of NOD mice to stimulate nitric oxide in both peritoneal and glandular macrophage pools to a similar extent as lipopolysaccharide + IFN-γ. VIP was not effective to prevent nitrite accumulation and modestly increased IL-10 levels in macrophages coincubated with acinar cells. An enhanced nitrite response of NOD glandular macrophages in basal and stimulated conditions compared to peritoneal cells is also shown. Copyright © 2007 S. Karger AG.
format JOUR
author Calafat, M.
Larocca, L.
Roca, V.
Pérez Leirós, C.
author_facet Calafat, M.
Larocca, L.
Roca, V.
Pérez Leirós, C.
author_sort Calafat, M.
title NOD mice exocrinopathy: Towards a neuroimmune link
title_short NOD mice exocrinopathy: Towards a neuroimmune link
title_full NOD mice exocrinopathy: Towards a neuroimmune link
title_fullStr NOD mice exocrinopathy: Towards a neuroimmune link
title_full_unstemmed NOD mice exocrinopathy: Towards a neuroimmune link
title_sort nod mice exocrinopathy: towards a neuroimmune link
url http://hdl.handle.net/20.500.12110/paper_10217401_v14_n3-4_p175_Calafat
work_keys_str_mv AT calafatm nodmiceexocrinopathytowardsaneuroimmunelink
AT laroccal nodmiceexocrinopathytowardsaneuroimmunelink
AT rocav nodmiceexocrinopathytowardsaneuroimmunelink
AT perezleirosc nodmiceexocrinopathytowardsaneuroimmunelink
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